Åsa Johansson

Contemporary menopausal hormone therapy and risk of cardiovascular disease - a Swedish nationwide register-based emulated target trial

Johansson, Therese; Karlsson, Torgny; Bliuc, Dana; Schmitz, Daniel et al.

Ingår i The BMJ, 2024

• DOI för Contemporary menopausal hormone therapy and risk of cardiovascular disease - a Swedish nationwide register-based emulated target trial
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Genotyping oral contraceptive users for venous thromboembolism risk

Lo Faro, Valeria; Johansson, Åsa

Ingår i American Journal of Obstetrics and Gynecology, 2024

• DOI för Genotyping oral contraceptive users for venous thromboembolism risk

The risk of venous thromboembolism in oral contraceptive users: the role of genetic factors-a prospective cohort study of 240,000 women in the UK Biobank

Lo Faro, Valeria; Johansson, Therese; Johansson, Åsa

Ingår i American Journal of Obstetrics and Gynecology, 2024

• DOI för The risk of venous thromboembolism in oral contraceptive users: the role of genetic factors-a prospective cohort study of 240,000 women in the UK Biobank
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The genetic landscape of neuro-related proteins in human plasma.

Repetto, Linda; Chen, Jiantao; Yang, Zhijian; Zhai, Ranran et al.

Ingår i Nature Human Behaviour, 2024

• DOI för The genetic landscape of neuro-related proteins in human plasma.

Copy number variations and their effect on the plasma proteome

Schmitz, Daniel; Li, Zhiwei; Lo Faro, Valeria; Rask-Andersen, Mathias et al.

Ingår i Genetics, 2023

• DOI för Copy number variations and their effect on the plasma proteome
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Contemporary menopausal hormone therapy and risk of cardiovascular disease - a Swedish nationwide register-based emulated target trial

Johansson, Therese; Karlsson, Torgny; Bliuc, Dana; Schmitz, Daniel et al.

Ingår i The BMJ, 2024

• DOI för Contemporary menopausal hormone therapy and risk of cardiovascular disease - a Swedish nationwide register-based emulated target trial
• Ladda ner fulltext (pdf) av Contemporary menopausal hormone therapy and risk of cardiovascular disease - a Swedish nationwide register-based emulated target trial

Genotyping oral contraceptive users for venous thromboembolism risk

Lo Faro, Valeria; Johansson, Åsa

Ingår i American Journal of Obstetrics and Gynecology, 2024

• DOI för Genotyping oral contraceptive users for venous thromboembolism risk

The risk of venous thromboembolism in oral contraceptive users: the role of genetic factors-a prospective cohort study of 240,000 women in the UK Biobank

Lo Faro, Valeria; Johansson, Therese; Johansson, Åsa

Ingår i American Journal of Obstetrics and Gynecology, 2024

• DOI för The risk of venous thromboembolism in oral contraceptive users: the role of genetic factors-a prospective cohort study of 240,000 women in the UK Biobank
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The genetic landscape of neuro-related proteins in human plasma.

Repetto, Linda; Chen, Jiantao; Yang, Zhijian; Zhai, Ranran et al.

Ingår i Nature Human Behaviour, 2024

• DOI för The genetic landscape of neuro-related proteins in human plasma.

Copy number variations and their effect on the plasma proteome

Schmitz, Daniel; Li, Zhiwei; Lo Faro, Valeria; Rask-Andersen, Mathias et al.

Ingår i Genetics, 2023

• DOI för Copy number variations and their effect on the plasma proteome
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Population-based cohort study of oral contraceptive use and risk of depression

Johansson, Therese; Vinther Larsen, S.; Bui, M.; Ek, Weronica E. et al.

Ingår i Epidemiology and Psychiatric Sciences, 2023

• DOI för Population-based cohort study of oral contraceptive use and risk of depression
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Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets

Zhao, Jing Hua; Stacey, David; Eriksson, Niclas; Macdonald-Dunlop, Erin et al.

Ingår i Nature Immunology, s. 1540-1551, 2023

• DOI för Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets
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Body Mass Index and the Risk of Rheumatic Disease: Linear and Nonlinear Mendelian Randomization Analyses

Karlsson, Torgny; Hadizadeh, Fatemeh; Rask-Andersen, Mathias; Johansson, Åsa et al.

Ingår i Arthritis & Rheumatology, s. 2027-2035, 2023

• DOI för Body Mass Index and the Risk of Rheumatic Disease: Linear and Nonlinear Mendelian Randomization Analyses
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Effects of oral contraceptives and menopausal hormone therapy on the risk of rheumatoid arthritis: a prospective cohort study

Hadizadeh, Fatemeh; Johansson, Therese; Johansson, Åsa; Karlsson, Torgny et al.

Ingår i Rheumatology, s. 2101-2108, 2023

• DOI för Effects of oral contraceptives and menopausal hormone therapy on the risk of rheumatoid arthritis: a prospective cohort study
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Genetic insights into resting heart rate and its role in cardiovascular disease

van de Vegte, Yordi; Eppinga, Ruben P.; van der Ende, M. Yldau; Hagemeijer, Yanick et al.

Ingår i Nature Communications, 2023

• DOI för Genetic insights into resting heart rate and its role in cardiovascular disease
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An atlas of genetic scores to predict multi-omic traits

Xu, Yu; Ritchie, Scott C; Liang, Yujian; Timmers, Paul R H J et al.

Ingår i Nature, s. 123-131, 2023

• DOI för An atlas of genetic scores to predict multi-omic traits

Adiposity and sex-specific cancer risk.

Rask-Andersen, Mathias; Ivansson, Emma; Höglund, Julia; Ek, Weronica E. et al.

Ingår i Cancer Cell, s. 1186-11970000, 2023

• DOI för Adiposity and sex-specific cancer risk.
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Forensic prediction of sex, age, height, body mass index, hip-to-waist ratio, smoking status and lipid lowering drugs using epigenetic markers and plasma proteins

Llobet, Mònica Ortega; Johansson, Åsa; Gyllensten, Ulf B.; Allen, Marie et al.

Ingår i Forensic Science International, 2023

• DOI för Forensic prediction of sex, age, height, body mass index, hip-to-waist ratio, smoking status and lipid lowering drugs using epigenetic markers and plasma proteins
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Building a precision medicine infrastructure at a national level: The Swedish experience.

Edsjö, Anders; Lindstrand, Anna; Gisselsson, David; Mölling, Paula et al.

Ingår i Cambridge prisms. Precision medicine, 2023

• DOI för Building a precision medicine infrastructure at a national level: The Swedish experience.

Precision medicine in complex diseases-Molecular subgrouping for improved prediction and treatment stratification.

Johansson, Åsa; Andreassen, Ole A; Brunak, Søren; Franks, Paul W et al.

Ingår i Journal of Internal Medicine, s. 378-396, 2023

• DOI för Precision medicine in complex diseases-Molecular subgrouping for improved prediction and treatment stratification.
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Polygenic risk scores and risk stratification in deep vein thrombosis.

Lo Faro, Valeria; Johansson, Therese; Höglund, Julia; Hadizadeh, Fatemeh et al.

Ingår i Thrombosis Research, s. 151-162, 2023

• DOI för Polygenic risk scores and risk stratification in deep vein thrombosis.

Illuminating the 'healthy obese' phenotype

Rask-Andersen, Mathias; Johansson, Åsa

Ingår i Nature Metabolism, s. 193-194, 2023

• DOI för Illuminating the 'healthy obese' phenotype

A multi-omics study of circulating phospholipid markers of blood pressure

Liu, Jun; de Vries, Paul S.; Del Greco, Fabiola M.; Johansson, Åsa et al.

Ingår i Scientific Reports, 2022

• DOI för A multi-omics study of circulating phospholipid markers of blood pressure
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Genetic Landscape of the ACE2 Coronavirus Receptor

Yang, Zhijian; Macdonald-Dunlop, Erin; Chen, Jiantao; Zhai, Ranran et al.

Ingår i Circulation, s. 1398-1411, 2022

• DOI för Genetic Landscape of the ACE2 Coronavirus Receptor
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Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

Wang, Zhe; Emmerich, Andrew; Pillon, Nicolas J; Moore, Tim et al.

Ingår i Nature Genetics, s. 1332-1344, 2022

• DOI för Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
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Gene-based variant analysis of whole-exome sequencing in relation to eosinophil count

Höglund, Julia; Hadizadeh, Fatemeh; Ek, Weronica E.; Karlsson, Torgny et al.

Ingår i Frontiers in Immunology, 2022

• DOI för Gene-based variant analysis of whole-exome sequencing in relation to eosinophil count
• Ladda ner fulltext (pdf) av Gene-based variant analysis of whole-exome sequencing in relation to eosinophil count

Contribution of rare whole-genome sequencing variants to plasma protein levels and the missing heritability

Kierczak, Marcin; Rafati, Nima; Höglund, Julia; Gourlé, Hadrien et al.

Ingår i Nature Communications, 2022

• DOI för Contribution of rare whole-genome sequencing variants to plasma protein levels and the missing heritability
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Oral Contraceptives, Hormone Replacement Therapy, and Stroke Risk

Johansson, Therese; Fowler, Philip; Ek, Weronica E.; Skalkidou, Alkistis et al.

Ingår i Stroke, s. 3107-3115, 2022

• DOI för Oral Contraceptives, Hormone Replacement Therapy, and Stroke Risk

Investigating the Effect of Estradiol Levels on the Risk of Breast, Endometrial, and Ovarian Cancer

Johansson, Åsa; Schmitz, Daniel; Höglund, Julia; Hadizadeh, Fatemeh et al.

Ingår i Journal of the Endocrine Society, 2022

• DOI för Investigating the Effect of Estradiol Levels on the Risk of Breast, Endometrial, and Ovarian Cancer
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Implementing precision medicine in a regionally organized healthcare system in Sweden.

Fioretos, Thoas; Wirta, Valtteri; Cavelier, Lucia; Berglund, Eva et al.

Ingår i Nature Medicine, s. 1980-1982, 2022

• DOI för Implementing precision medicine in a regionally organized healthcare system in Sweden.

Causal effects of inflammatory protein biomarkers on inflammatory diseases

Ek, Weronica E; Karlsson, Torgny; Höglund, Julia; Rask-Andersen, Mathias et al.

Ingår i Science Advances, 2021

• DOI för Causal effects of inflammatory protein biomarkers on inflammatory diseases
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Inflammation-related plasma protein levels and association with adiposity measurements in young adults

Klevebro, Susanna; Björkander, Sophia; Ekström, Sandra; Merid, Simon K. et al.

Ingår i Scientific Reports, 2021

• DOI för Inflammation-related plasma protein levels and association with adiposity measurements in young adults
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DNA methylation in cord blood in association with prenatal depressive symptoms

Kunovac Kallak, Theodora; Bränn, Emma; Fransson, Emma; Johansson, Åsa et al.

Ingår i Clinical Epigenetics, 2021

• DOI för DNA methylation in cord blood in association with prenatal depressive symptoms
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Modification of Heritability for Educational Attainment and Fluid Intelligence by Socioeconomic Deprivation in the UK Biobank

Rask-Andersen, Mathias; Karlsson, Torgny; Ek, Weronica E; Johansson, Asa

Ingår i American Journal of Psychiatry, s. 625-634, 2021

• DOI för Modification of Heritability for Educational Attainment and Fluid Intelligence by Socioeconomic Deprivation in the UK Biobank

Immune cells lacking Y chromosome show dysregulation of autosomal gene expression

Dumanski, Jan P.; Halvardson, Jonatan; Davies, Hanna; Rychlicka-Buniowska, Edyta et al.

Ingår i Cellular and Molecular Life Sciences (CMLS), s. 4019-4033, 2021

• DOI för Immune cells lacking Y chromosome show dysregulation of autosomal gene expression
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Characterization of the human ABO genotypes and their association to common inflammatory and cardiovascular diseases in the UK Biobank

Höglund, Julia; Karlsson, Torgny; Johansson, Therese; Ek, Weronica E. et al.

Ingår i American Journal of Hematology, s. 1350-1362, 2021

• DOI för Characterization of the human ABO genotypes and their association to common inflammatory and cardiovascular diseases in the UK Biobank
• Ladda ner fulltext (pdf) av Characterization of the human ABO genotypes and their association to common inflammatory and cardiovascular diseases in the UK Biobank

A combined genome-wide association and molecular study of age-related hearing loss in H. sapiens

Liu, Wei; Johansson, Åsa; Rask-Andersen, Helge; Rask-Andersen, Mathias

Ingår i BMC Medicine, 2021

• DOI för A combined genome-wide association and molecular study of age-related hearing loss in H. sapiens
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Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19

Klaric, Lucija; Gisby, Jack S; Papadaki, Artemis; Muckian, Marisa D et al.

Ingår i medRxiv : the preprint server for health sciences, s. 1-28, 2021

• DOI för Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19

Time-dependent effects of oral contraceptive use on breast, ovarian and endometrial cancers

Karlsson, Torgny; Johansson, Therese; Höglund, Julia; Ek, Weronica E et al.

Ingår i Cancer Research, s. 1153-1162, 2021

• DOI för Time-dependent effects of oral contraceptive use on breast, ovarian and endometrial cancers

Genome-Wide Association Study of Estradiol Levels and the Causal Effect of Estradiol on Bone Mineral Density

Schmitz, Daniel; Ek, Weronica E.; Berggren, Elin; Höglund, Julia et al.

Ingår i Journal of Clinical Endocrinology and Metabolism, 2021

• DOI för Genome-Wide Association Study of Estradiol Levels and the Causal Effect of Estradiol on Bone Mineral Density
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Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals

Folkersen, Lasse; Gustafsson, Stefan; Wang, Qin; Hvidberg Hansen, Daniel et al.

Ingår i Nature Metabolism, s. 1135-1148, 2020

• DOI för Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals

Improved power and precision with whole genome sequencing data in genome-wide association studies of inflammatory biomarkers

Höglund, Julia; Rafati, Nima; Rask-Andersen, Mathias; Enroth, Stefan et al.

Ingår i Scientific Reports, 2019

• DOI för Improved power and precision with whole genome sequencing data in genome-wide association studies of inflammatory biomarkers
• Ladda ner fulltext (pdf) av Improved power and precision with whole genome sequencing data in genome-wide association studies of inflammatory biomarkers

Associations of autozygosity with a broad range of human phenotypes

Clark, David W.; Karlsson, Torgny; Sennblad, Bengt; Gyllensten, Ulf B. et al.

Ingår i Nature Communications, 2019

• DOI för Associations of autozygosity with a broad range of human phenotypes
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Contribution of genetics to visceral adiposity and its relation to cardiovascular and metabolic disease.

Karlsson, Torgny; Rask-Andersen, Mathias; Pan, Gang; Höglund, Julia et al.

Ingår i Nature Medicine, s. 1390-1395, 2019

• DOI för Contribution of genetics to visceral adiposity and its relation to cardiovascular and metabolic disease.

Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects

Rask-Andersen, Mathias; Karlsson, Torgny; Ek, Weronica E; Johansson, Åsa

Ingår i Nature Communications, 2019

• DOI för Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects
• Ladda ner fulltext (pdf) av Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects

Genome-wide association analysis of 350 000 Caucasians from the UK Biobank identifies novel loci for asthma, hay fever and eczema

Johansson, Åsa; Rask-Andersen, Mathias; Karlsson, Torgny; Ek, Weronica E

Ingår i Human Molecular Genetics, s. 4022-4041, 2019

• DOI för Genome-wide association analysis of 350 000 Caucasians from the UK Biobank identifies novel loci for asthma, hay fever and eczema
• Ladda ner fulltext (pdf) av Genome-wide association analysis of 350 000 Caucasians from the UK Biobank identifies novel loci for asthma, hay fever and eczema

Epigenome-wide association study of lung function level and its change

Imboden, Medea; Wielscher, Matthias; Rezwan, Faisal I; Amaral, André F S et al.

Ingår i European Respiratory Journal, 2019

• DOI för Epigenome-wide association study of lung function level and its change
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A Meta-Analysis of Genome-Wide Association Studies of Growth Differentiation Factor-15 Concentration in Blood

Jiang, Jiyang; Thalamuthu, Anbupalam; Ho, Jennifer E.; Mahajan, Anubha et al.

Ingår i Frontiers in Genetics, 2018

• DOI för A Meta-Analysis of Genome-Wide Association Studies of Growth Differentiation Factor-15 Concentration in Blood
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Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.

Evangelou, Evangelos; Warren, Helen R; Mosen-Ansorena, David; Mifsud, Borbala et al.

Ingår i Nature Genetics, s. 1412-1425, 2018

• DOI för Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.

Meta-analysis of exome array data identifies six novel genetic loci for lung function.

Jackson, Victoria E; Latourelle, Jeanne C; Wain, Louise V; Smith, Albert V et al.

Ingår i Wellcome open research, 2018

• DOI för Meta-analysis of exome array data identifies six novel genetic loci for lung function.

Genetic variants influencing phenotypic variance heterogeneity

Ek, Weronica E; Rask-Andersen, Mathias; Karlsson, Torgny; Enroth, Stefan et al.

Ingår i Human Molecular Genetics, s. 799-810, 2018

• DOI för Genetic variants influencing phenotypic variance heterogeneity

Systemic and specific effects of antihypertensive and lipid-lowering medication on plasma protein biomarkers for cardiovascular diseases

Enroth, Stefan; Maturi, Varun; Berggrund, Malin; Bosdotter Enroth, Sofia et al.

Ingår i Scientific Reports, 2018

• DOI för Systemic and specific effects of antihypertensive and lipid-lowering medication on plasma protein biomarkers for cardiovascular diseases
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Breast-feeding and risk of asthma, hay fever, and eczema

Ek, Weronica E; Karlsson, Torgny; Hernándes, Carlos Azuaje; Rask-Andersen, Mathias et al.

Ingår i Journal of Allergy and Clinical Immunology, s. 1157-+, 2018

• DOI för Breast-feeding and risk of asthma, hay fever, and eczema

Epigenome-wide DNA methylation study of IgE concentration in relation to self-reported allergies

Ek, Weronica E.; Ahsan, Muhammad; Rask-Andersen, Mathias; Liang, Liming et al.

Ingår i Epigenomics, s. 407-418, 2017

• DOI för Epigenome-wide DNA methylation study of IgE concentration in relation to self-reported allergies

Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

Wain, Louise V.; Vaez, Ahmad; Jansen, Rick; Joehanes, Roby et al.

Ingår i Hypertension, 2017

• DOI för Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

Genome-wide physical activity interactions in adiposity: A meta-analysis of 200,452 adults.

Graff, Mariaelisa; Scott, Robert A; Justice, Anne E; Young, Kristin L et al.

Ingår i PLOS Genetics, 2017

• DOI för Genome-wide physical activity interactions in adiposity: A meta-analysis of 200,452 adults.
• Ladda ner fulltext (pdf) av Genome-wide physical activity interactions in adiposity: A meta-analysis of 200,452 adults.

1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.

Gorski, Mathias; van der Most, Peter J; Teumer, Alexander; Chu, Audrey Y et al.

Ingår i Scientific Reports, 2017

• DOI för 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
• Ladda ner fulltext (pdf) av 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.

Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease

Folkersen, Lasse; Fauman, Eric; Sabater-Lleal, Maria; Strawbridge, Rona J et al.

Ingår i PLOS Genetics, 2017

• DOI för Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease
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Gene-environment interaction study for BMI reveals interactions between genetic factors and physical activity, alcohol consumption and socioeconomic status.

Rask-Andersen, Mathias; Karlsson, Torgny; Ek, Weronica E; Johansson, Åsa

Ingår i PLOS Genetics, 2017

• DOI för Gene-environment interaction study for BMI reveals interactions between genetic factors and physical activity, alcohol consumption and socioeconomic status.
• Ladda ner fulltext (pdf) av Gene-environment interaction study for BMI reveals interactions between genetic factors and physical activity, alcohol consumption and socioeconomic status.

The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases.

Ahsan, Muhammad; Ek, Weronica E; Rask-Andersen, Mathias; Karlsson, Torgny et al.

Ingår i PLOS Genetics, 2017

• DOI för The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases.
• Ladda ner fulltext (pdf) av The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases.

SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population

Ameur, Adam; Dahlberg, Johan; Olason, Pall; Vezzi, Francesco et al.

Ingår i European Journal of Human Genetics, s. 1253-1260, 2017

• DOI för SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population
• Ladda ner fulltext (pdf) av SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population

Tea and coffee consumption in relation to DNA methylation in four European cohorts

Ek, Weronica E.; Tobi, Elmar W; Ahsan, Muhammad; Lampa, Erik et al.

Ingår i Human Molecular Genetics, s. 3221-3231, 2017

• DOI för Tea and coffee consumption in relation to DNA methylation in four European cohorts

Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

Warren, Helen R.; Evangelou, Evangelos; Cabrera, Claudia P.; Gao, He et al.

Ingår i Nature Genetics, s. 403-415, 2017

• DOI för Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

A multiple-phenotype imputation method for genetic studies

Dahl, Andrew; Iotchkova, Valentina; Baud, Amelie; Johansson, Åsa et al.

Ingår i Nature Genetics, s. 466-472, 2016

• DOI för A multiple-phenotype imputation method for genetic studies

The role of DNA methylation in the pathogenesis of disease: what can epigenome-wide association studies tell?

Ek, Weronica E; Rask-Andersen, Mathias; Johansson, Åsa

Ingår i Epigenomics, s. 5-7, 2016

• DOI för The role of DNA methylation in the pathogenesis of disease: what can epigenome-wide association studies tell?

Genome-wide DNA methylation study identifies genes associated with the cardiovascular biomarker GDF-15

Ek, Weronica E; Hedman, Åsa K; Enroth, Stefan; Morris, Andrew P et al.

Ingår i Human Molecular Genetics, s. 817-827, 2016

• DOI för Genome-wide DNA methylation study identifies genes associated with the cardiovascular biomarker GDF-15

Epigenome-wide association study reveals differential DNA methylation in individuals with a history of myocardial infarction

Rask-Andersen, Mathias; Martinsson, David; Ahsan, Muhammad; Enroth, Stefan et al.

Ingår i Human Molecular Genetics, s. 4739-4748, 2016

• DOI för Epigenome-wide association study reveals differential DNA methylation in individuals with a history of myocardial infarction

Genome-wide association and Mendelian randomization study of NT-proBNP in patients with acute coronary syndrome

Johansson, Åsa; Eriksson, Niclas; Lindholm, Daniel; Varenhorst, Christoph et al.

Ingår i Human Molecular Genetics, s. 1447-1456, 2016

• DOI för Genome-wide association and Mendelian randomization study of NT-proBNP in patients with acute coronary syndrome

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Pattaro, Cristian; Teumer, Alexander; Gorski, Mathias; Chu, Audrey Y et al.

Ingår i Nature Communications, 2016

• DOI för Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
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KLB is associated with alcohol drinking, and its gene product beta-Klotho is necessary for FGF21 regulation of alcohol preference

Schumann, Gunter; Liu, Chunyu; O'Reilly, Paul; Gao, He et al.

Ingår i Proceedings of the National Academy of Sciences of the United States of America, s. 14372-14377, 2016

• DOI för KLB is associated with alcohol drinking, and its gene product beta-Klotho is necessary for FGF21 regulation of alcohol preference

Protein profiling reveals consequences of lifestyle choices on predicted biological aging

Enroth, Stefan; Enroth, Sofia Bosdotter; Johansson, Åsa; Gyllensten, Ulf

Ingår i Scientific Reports, 2015

• DOI för Protein profiling reveals consequences of lifestyle choices on predicted biological aging

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

Winkler, Thomas W.; Justice, Anne E.; Graff, Mariaelisa; Barata, Llilda et al.

Ingår i PLOS Genetics, 2015

• DOI för The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
• Ladda ner fulltext (pdf) av The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans

Huffman, Jennifer E.; Albrecht, Eva; Teumer, Alexander; Mangino, Massimo et al.

Ingår i PLOS ONE, 2015

• DOI för Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans
• Ladda ner fulltext (pdf) av Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans

Homozygous loss-of-function variants in European cosmopolitan and isolate populations

Kaiser, Vera B; Svinti, Victoria; Prendergast, James G; Chau, You-Ying et al.

Ingår i Human Molecular Genetics, s. 5464-5475, 2015

• DOI för Homozygous loss-of-function variants in European cosmopolitan and isolate populations
• Ladda ner fulltext (pdf) av Homozygous loss-of-function variants in European cosmopolitan and isolate populations

NLRC4 Inflammasome Is an Important Regulator of Interleukin-18 Levels in Patients With Acute Coronary Syndromes Genome-Wide Association Study in the PLATelet inhibition and patient Outcomes Trial (PLATO)

Johansson, Åsa; Eriksson, Niclas; Becker, Richard C.; Storey, Robert F. et al.

Ingår i Circulation, s. 498-506, 2015

• DOI för NLRC4 Inflammasome Is an Important Regulator of Interleukin-18 Levels in Patients With Acute Coronary Syndromes Genome-Wide Association Study in the PLATelet inhibition and patient Outcomes Trial (PLATO)

Effect of genetic variations on ticagrelor plasma levels and clinical outcomes

Varenhorst, Christoph; Eriksson, Niclas; Johansson, Åsa; Barratt, Bryan J. et al.

Ingår i European Heart Journal, s. 1901-1912, 2015

• DOI för Effect of genetic variations on ticagrelor plasma levels and clinical outcomes

Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation

Soler Artigas, María; Wain, Louise V; Miller, Suzanne; Kheirallah, Abdul Kader et al.

Ingår i Nature Communications, 2015

• DOI för Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation
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Protein profiling reveals consequences of lifestyle choices on predicted biological aging

Enroth, Stefan; Enroth, Sofia Bosdotter; Johansson, Åsa; Gyllensten, Ulf

Ingår i Scientific Reports, 2015

• DOI för Protein profiling reveals consequences of lifestyle choices on predicted biological aging

Genetic studies of body mass index yield new insights for obesity biology

Locke, Adam E; Kahali, Bratati; Berndt, Sonja I; Justice, Anne E et al.

Ingår i Nature, s. 197-206, 2015

• DOI för Genetic studies of body mass index yield new insights for obesity biology

Genome-Wide Association Study Identifies That the ABO Blood Group System Influences Interleukin-10 Levels and the Risk of Clinical Events in Patients with Acute Coronary Syndrome

Johansson, Åsa; Alfredsson, Jenny; Eriksson, Niclas; Wallentin, Lars et al.

Ingår i PLOS ONE, 2015

• DOI för Genome-Wide Association Study Identifies That the ABO Blood Group System Influences Interleukin-10 Levels and the Risk of Clinical Events in Patients with Acute Coronary Syndrome
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Effect of genetic and environmental factors on protein biomarkers for common non-communicable disease and use of personally normalized plasma protein profiles (PNPPP)

Enroth, Stefan; Enroth, Sofia Bosdotter; Johansson, Åsa; Gyllensten, Ulf

Ingår i Biomarkers, s. 355-364, 2015

• DOI för Effect of genetic and environmental factors on protein biomarkers for common non-communicable disease and use of personally normalized plasma protein profiles (PNPPP)

Directional dominance on stature and cognition in diverse human populations

Joshi, Peter K; Esko, Tonu; Mattsson, Hannele; Eklund, Niina et al.

Ingår i Nature, s. 459-462, 2015

• DOI för Directional dominance on stature and cognition in diverse human populations

Defining the role of common variation in the genomic and biological architecture of adult human height

Wood, Andrew R; Esko, Tonu; Yang, Jian; Vedantam, Sailaja et al.

Ingår i Nature Genetics, s. 1173-1186, 2014

• DOI för Defining the role of common variation in the genomic and biological architecture of adult human height

Genome-wide association analysis identifies six new loci associated with forced vital capacity

Loth, Daan W; Artigas, María Soler; Gharib, Sina A; Wain, Louise V et al.

Ingår i Nature Genetics, s. 669-677, 2014

• DOI för Genome-wide association analysis identifies six new loci associated with forced vital capacity

Polymorphism of the cystatin C gene in patients with acute coronary syndromes: Results from the PLATelet Inhibition and Patient Outcomes (PLATO) Study

Åkerblom, Axel; Eriksson, Niclas; Wallentin, Lars; Siegbahn, Agneta et al.

Ingår i American Heart Journal, s. 96-102, 2014

• DOI för Polymorphism of the cystatin C gene in patients with acute coronary syndromes: Results from the PLATelet Inhibition and Patient Outcomes (PLATO) Study

Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs

Enroth, Stefan; Johansson, Åsa; Bosdotter Enroth, Sofia; Gyllensten, Ulf

Ingår i Nature Communications, s. 4684, 2014

• DOI för Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs

Smoke-related DNA methylation changes in the etiology of human disease

Besingi, Welisane; Johansson, Åsa

Ingår i Human Molecular Genetics, s. 2290-2297, 2014

• DOI för Smoke-related DNA methylation changes in the etiology of human disease

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Berndt, Sonja I.; Gustafsson, Stefan; Maegi, Reedik; Ganna, Andrea et al.

Ingår i Nature Genetics, s. 501-U69, 2013

• DOI för Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
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Prevalence and sensitization of atopic allergy and coeliac disease in the Northern Sweden Population Health Study

Enroth, Stefan; Dahlbom, Ingrid; Hansson, Tony; Johansson, Åsa et al.

Ingår i International Journal of Circumpolar Health, s. 21403, 2013

• DOI för Prevalence and sensitization of atopic allergy and coeliac disease in the Northern Sweden Population Health Study
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Common variants associated with plasma triglycerides and risk for coronary artery disease

Do, Ron; Willer, Cristen J.; Schmidt, Ellen M.; Sengupta, Sebanti et al.

Ingår i Nature Genetics, s. 1345-+, 2013

• DOI för Common variants associated with plasma triglycerides and risk for coronary artery disease

Discovery and refinement of loci associated with lipid levels

Willer, Cristen J.; Schmidt, Ellen M.; Sengupta, Sebanti; Peloso, Gina M. et al.

Ingår i Nature Genetics, s. 1274-1283, 2013

• DOI för Discovery and refinement of loci associated with lipid levels

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

Koettgen, Anna; Albrecht, Eva; Teumer, Alexander; Vitart, Veronique et al.

Ingår i Nature Genetics, s. 145-154, 2013

• DOI för Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

Are There Any Causal Relations Between Growth Differentiation Factor 15 and Outcomes in Patients With Acute Coronary Syndrome?: - A Report From the Plato Gwas Study

Hagström, Emil; Eriksson, Niclas; Johansson, Åsa; Bertilsson, Maria et al.

Ingår i Circulation, 2013

Differential Gene Expression at the Maternal-Fetal Interface in Preeclampsia Is Influenced by Gestational Age

Lian, Ingrid A.; Langaas, Mette; Moses, Eric; Johansson, Åsa

Ingår i PLOS ONE, 2013

• DOI för Differential Gene Expression at the Maternal-Fetal Interface in Preeclampsia Is Influenced by Gestational Age
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Continuous Aging of the Human DNA Methylome Throughout the Human Lifespan

Johansson, Åsa; Enroth, Stefan; Gyllensten, Ulf

Ingår i PLOS ONE, 2013

• DOI för Continuous Aging of the Human DNA Methylome Throughout the Human Lifespan
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Omega-3 and omega-6 fatty acids are more efficiently synthesized in populations having a high frequency of the derived FADS-haplotype

Enroth, Stefan; Ameur, Adam; Johansson, Åsa; Gyllensten, Ulf

Ingår i International Journal of Circumpolar Health, s. 511-512, 2013

Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits

Randall, Joshua C.; Winkler, Thomas W.; Kutalik, Zoltan; Berndt, Sonja I. et al.

Ingår i PLOS Genetics, 2013

• DOI för Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits
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Evaluation of the Effect of Interleukin 18 Associated Genetic Polymorphisms on Risk of Cardiovascular Events in Patients With Acute Coronary Syndrome

Siegbahn, Agneta; Johansson, Åsa; Eriksson, Niclas; Hagström, Emil et al.

Ingår i Circulation, 2013

Genetic Polymorphism and Relationship to Cystatin C Concentrations and Outcome - Results From the Platelet Inhibition and Patient Outcomes Study

Åkerblom, Axel; Wallentin, Lars; Siegbahn, Agneta; Becker, Richard C. et al.

Ingår i Circulation, 2013

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

den Hoed, Marcel; Eijgelsheim, Mark; Esko, Tonu; Brundel, Bianca J. J. M. et al.

Ingår i Nature Genetics, s. 621-+, 2013

• DOI för Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

Identification of genetic variants influencing the human plasma proteome

Johansson, Åsa; Enroth, Stefan; Palmblad, Magnus; Deelder, Andre M. et al.

Ingår i Proceedings of the National Academy of Sciences of the United States of America, s. 4673-4678, 2013

• DOI för Identification of genetic variants influencing the human plasma proteome

Large-scale association analysis identifies new risk loci for coronary artery disease

Deloukas, Panos; Kanoni, Stavroula; Willenborg, Christina; Farrall, Martin et al.

Ingår i Nature Genetics, s. 25-33, 2013

• DOI för Large-scale association analysis identifies new risk loci for coronary artery disease

Animal source food intake and association with blood cholesterol, glycerophospholipids and sphingolipids in a northern Swedish population

Igl, Wilmar; Kamal-Eldin, Afaf; Johansson, Asa; Liebisch, Gerhard et al.

Ingår i International Journal of Circumpolar Health, s. 421-427, 2013

• DOI för Animal source food intake and association with blood cholesterol, glycerophospholipids and sphingolipids in a northern Swedish population
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Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal Function

Parsa, Afshin; Fuchsberger, Christian; Koettgen, Anna; O'Seaghdha, Conall M. et al.

Ingår i Journal of the American Society of Nephrology, s. 2105-2117, 2013

• DOI för Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal Function

Assessing The Effects Of Climate Change On Health And Lifestyle In Sub-Arctic Areas In Sweden - The Northern Sweden Population Health Study

Gyllensten, Ulf; Johansson, Åsa; Enroth, Stefan; Jonasson, Inger

Ingår i International Journal of Circumpolar Health, s. 516-517, 2013

Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function

Pattaro, Cristian; Koettgen, Anna; Teumer, Alexander; Garnaas, Maija et al.

Ingår i PLoS Genetics, 2012

• DOI för Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function
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Genetic Adaptation of Fatty-Acid Metabolism: A Human-Specific Haplotype Increasing the Biosynthesis of Long-Chain Omega-3 and Omega-6 Fatty Acids

Ameur, Adam; Enroth, Stefan; Johansson, Åsa; Zaboli, Ghazal et al.

Ingår i American Journal of Human Genetics, s. 809-820, 2012

• DOI för Genetic Adaptation of Fatty-Acid Metabolism: A Human-Specific Haplotype Increasing the Biosynthesis of Long-Chain Omega-3 and Omega-6 Fatty Acids

Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations

Demirkan, Ayse; van Duijn, Cornelia M.; Ugocsai, Peter; Isaacs, Aaron et al.

Ingår i PLoS Genetics, 2012

• DOI för Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations
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Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

Chasman, Daniel I.; Fuchsberger, Christian; Pattaro, Cristian; Teumer, Alexander et al.

Ingår i Human Molecular Genetics, s. 5329-5343, 2012

• DOI för Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

Evidence of Inbreeding Depression on Human Height

McQuillan, Ruth; Eklund, Niina; Pirastu, Nicola; Kuningas, Maris et al.

Ingår i PLOS Genetics, 2012

• DOI för Evidence of Inbreeding Depression on Human Height
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Polymorphisms in sh2b1 and spns1 loci are associated with triglyceride levels in a healthy population in northern Sweden

Västermark, Åke; Jacobsson, Josefin; Johansson, Åsa; Fredriksson, Robert et al.

Ingår i Journal of Genetics, s. 237-240, 2012

• DOI för Polymorphisms in sh2b1 and spns1 loci are associated with triglyceride levels in a healthy population in northern Sweden

Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits

Zaboli, Ghazal; Ameur, Adam; Igl, Wilmar; Johansson, Åsa et al.

Ingår i European Journal of Human Genetics, s. 77-83, 2012

• DOI för Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits

A Comprehensive Evaluation of Potential Lung Function Associated Genes in the SpiroMeta General Population Sample

Obeidat, Ma'en; Wain, Louise V.; Shrine, Nick; Kalsheker, Noor et al.

Ingår i PLOS ONE, 2011

• DOI för A Comprehensive Evaluation of Potential Lung Function Associated Genes in the SpiroMeta General Population Sample

Genetic architecture of circulating lipid levels

Demirkan, Ayse; Amin, Najaf; Isaacs, Aaron; Jarvelin, Marjo-Riitta et al.

Ingår i European Journal of Human Genetics, s. 813-819, 2011

• DOI för Genetic architecture of circulating lipid levels

Partial correlation network analyses to detect altered gene interactions in human disease: using preeclampsia as a model

Johansson, Åsa; Løset, Mari; Mundal, Siv B; Johnson, Matthew P et al.

Ingår i Human Genetics, s. 25-34, 2011

• DOI för Partial correlation network analyses to detect altered gene interactions in human disease: using preeclampsia as a model

Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adults

Huffman, Jennifer E.; Knezevic, Ana; Vitart, Veronique; Kattla, Jayesh et al.

Ingår i Human Molecular Genetics, s. 5000-5011, 2011

• DOI för Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adults

A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol

Surakka, Ida; Isaacs, Aaron; Karssen, Lennart C.; Laurila, Pirkka-Pekka P. et al.

Ingår i PLoS Genetics, 2011

• DOI för A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol

Identification of ACOX2 as a shared genetic risk factor for preeclampsia and cardiovascular disease

Johansson, Åsa; Curran, Joanne E.; Johnson, Matthew P.; Freed, Katy A. et al.

Ingår i European Journal of Human Genetics, s. 796-800, 2011

• DOI för Identification of ACOX2 as a shared genetic risk factor for preeclampsia and cardiovascular disease

The Northern Swedish Population Health Study (NSPHS): a paradigmatic study in a rural population combining community health and basic research

Igl, Wilmar; Johansson, Åsa; Gyllensten, Ulf

Ingår i Rural and remote health, s. 1363, 2010

A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level

Pattaro, Cristian; De Grandi, Alessandro; Vitart, Veronique; Hayward, Caroline et al.

Ingår i BMC Medical Genetics, s. 41, 2010

• DOI för A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Heid, Iris M; Jackson, Anne U; Randall, Joshua C; Winkler, Thomas W et al.

Ingår i Nature Genetics, s. 949-960, 2010

• DOI för Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Hundreds of variants clustered in genomic loci and biological pathways affect human height

Allen, Hana Lango; Estrada, Karol; Lettre, Guillaume; Berndt, Sonja I. et al.

Ingår i Nature, s. 832-838, 2010

• DOI för Hundreds of variants clustered in genomic loci and biological pathways affect human height

Genome-wide association study identifies five loci associated with lung function

Repapi, Emmanouela; Sayers, Ian; Wain, Louise V.; Burton, Paul R. et al.

Ingår i Nature Genetics, s. 36-44, 2010

• DOI för Genome-wide association study identifies five loci associated with lung function

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

Speliotes, Elizabeth K.; Willer, Cristen J.; Berndt, Sonja I.; Monda, Keri L. et al.

Ingår i Nature Genetics, s. 937-948, 2010

• DOI för Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

New loci associated with kidney function and chronic kidney disease

Köttgen, Anna; Pattaro, Cristian; Böger, Carsten A.; Fuchsberger, Christian et al.

Ingår i Nature Genetics, s. 376-384, 2010

• DOI för New loci associated with kidney function and chronic kidney disease

Modeling of Environmental Effects in Genome-Wide Association Studies Identifies SLC2A2 and HP as Novel Loci Influencing Serum Cholesterol Levels

Igl, Wilmar; Johansson, Åsa; Wilson, James F.; Wild, Sarah H. et al.

Ingår i PLoS Genetics, 2010

• DOI för Modeling of Environmental Effects in Genome-Wide Association Studies Identifies SLC2A2 and HP as Novel Loci Influencing Serum Cholesterol Levels

Biological, clinical and population relevance of 95 loci for blood lipids

Teslovich, Tanya M.; Musunuru, Kiran; Smith, Albert V.; Edmondson, Andrew C. et al.

Ingår i Nature, s. 707-713, 2010

• DOI för Biological, clinical and population relevance of 95 loci for blood lipids

Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene

Johansson, Åsa; Marroni, Fabio; Hayward, Caroline; Franklin, Christopher S. et al.

Ingår i Obesity, s. 803-808, 2010

• DOI för Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene

Genes predict village of origin in rural Europe

O'Dushlaine, Colm; McQuillan, Ruth; Weale, Michael E.; Crouch, Daniel J. M. et al.

Ingår i European Journal of Human Genetics, s. 1269-1270, 2010

• DOI för Genes predict village of origin in rural Europe

STOX2 but not STOX1 is differentially expressed in decidua from pre-eclamptic women: data from the Second Nord-Trondelag Health Study

Fenstad, M H; Johnson, M P; Løset, M; Mundal, S B et al.

Ingår i Molecular human reproduction, s. 960-968, 2010

• DOI för STOX2 but not STOX1 is differentially expressed in decidua from pre-eclamptic women: data from the Second Nord-Trondelag Health Study

Extended haplotypes in the growth hormone releasing hormone receptor gene (GHRHR) are associated with normal variation in height

Johansson, Åsa; Jonasson, Inger; Gyllensten, Ulf

Ingår i PLOS ONE, 2009

• DOI för Extended haplotypes in the growth hormone releasing hormone receptor gene (GHRHR) are associated with normal variation in height

Genetic determinants of circulating sphingolipid concentrations in European populations

Hicks, Andrew A.; Pramstaller, Peter P.; Johansson, Åsa; Vitart, Veronique et al.

Ingår i PLoS genetics, 2009

• DOI för Genetic determinants of circulating sphingolipid concentrations in European populations

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

Aulchenko, Yurii S; Ripatti, Samuli; Lindqvist, Ida; Boomsma, Dorret et al.

Ingår i Nature Genetics, s. 47-55, 2009

• DOI för Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

Adherence to a traditional lifestyle affects food and nutrient intake among modern Swedish Sami

Ross, Alastair B; Johansson, Åsa; Vavruch-Nilsson, Veronika; Hassler, Sven et al.

Ingår i International Journal of Circumpolar Health, s. 372-385, 2009

Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations

Kolz, Melanie; Johnson, Toby; Sanna, Serena; Teumer, Alexander et al.

Ingår i PLoS genetics, 2009

• DOI för Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations

NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium

Heard-Costa, Nancy L; Zillikens, M Carola; Monda, Keri L; Johansson, Åsa et al.

Ingår i PLoS genetics, 2009

• DOI för NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium

Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis

Johansson, Åsa; Marroni, Fabio; Hayward, Caroline; Franklin, Christopher S. et al.

Ingår i Human Molecular Genetics, s. 373-380, 2009

• DOI för Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis

Identification of local selective sweeps in human populations since the exodus from Africa

Johansson, Åsa; Gyllensten, Ulf

Ingår i Hereditas, s. 126-137, 2008

• DOI för Identification of local selective sweeps in human populations since the exodus from Africa

Genetic origin of the Swedish Sami inferred from HLA class I and class II allele frequencies

Johansson, Åsa; Ingman, Max; Mack, Steven J; Erlich, Henry et al.

Ingår i European Journal of Human Genetics, s. 1341-1349, 2008

• DOI för Genetic origin of the Swedish Sami inferred from HLA class I and class II allele frequencies

Evaluation of the SNP tagging approach in an independent population sample: Array-based SNP discovery in Sami

Johansson, Åsa; Vavruch-Nilsson, Veronika; Cox, David; Frazer, Kelly et al.

Ingår i Human Genetics, s. 141-150, 2007

• DOI för Evaluation of the SNP tagging approach in an independent population sample: Array-based SNP discovery in Sami

Lifestyle, genetics, and disease in Sami.

Ross, Alastair B; Johansson, Asa; Ingman, Max; Gyllensten, Ulf

Ingår i Croat Med J, s. 553-65, 2006

Linkage disequilibrium between microsatellite markers in the Swedish Sami relative to a worldwide selection of populations

Johansson, Åsa; Vavruch-Nilsson, Veronika; Edin-Liljegren, Anette; Sjölander, Per et al.

Ingår i Human Genetics, s. 105-113, 2005

• DOI för Linkage disequilibrium between microsatellite markers in the Swedish Sami relative to a worldwide selection of populations

Linkage disequilibrium between microsatellite markers in the Swedish Sami relative to a worldwide selection of populations.

Johansson, Asa; Vavruch-Nilsson, Veronika; Edin-Liljegren, Anette; Sjölander, Per et al.

Ingår i Hum Genet, s. 105-13, 2005

A novel method for automatic genotyping of microsatellite markers based on parametric pattern recognition

Johansson, Åsa; Karlsson, Patrik; Gyllensten, Ulf

Ingår i Human Genetics, s. 316-324, 2003

• DOI för A novel method for automatic genotyping of microsatellite markers based on parametric pattern recognition

A novel method for automatic genotyping of microsatellite markers based on parametric pattern recognition.

Johansson, Åsa; Karlsson, P; Gyllensten, Ulf

Ingår i Hum Genet, s. 316, 2003

Technological readiness and implementation of genomic-driven precision medicine for complex diseases

Franks, P. W.; Melén, E.; Friedman, M.; Sundström, Johan et al.

Ingår i Journal of Internal Medicine, s. 602-620, 2021

• DOI för Technological readiness and implementation of genomic-driven precision medicine for complex diseases
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T2T-CHM13 improves read mapping and detection of clinically relevant variation

Schmitz, Daniel; Ameur, Adam; Johansson, Åsa